http://rdf.ncbi.nlm.nih.gov/pubchem/patent/TR-201902686-T4

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_2ca2e4410855da087e11bf3eea8933fa
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P35-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-4545
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-14
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-4545
filingDate 2015-11-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_09df9c3011f4014120ba3aef3cf9e923
publicationDate 2019-03-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber TR-201902686-T4
titleOfInvention Aurora A kinase inhibitor.
abstract The present invention includes (2S, 4S) -1 - [(3-chloro-2-fluoro-phenyl) methyl] -4 - [[3-fluoro-6 - [(5-methyl-1H-pyrazol-3-yl) amino ] -2-pyridyl] methyl] -2-methyl-piperidine-4-carboxylic acid (Formula 1) and (2R, 4R) -1 - [(3-chloro-2-fluoro-phenyl) methyl] -4- [[3-fluoro-6- [(5-methyl-1H-pyrazol-3-yl) amino] -2-pyridyl] methyl] -2-methyl-piperidine-4-carboxylic acid (Formula 2) or their pharmaceutical It provides an aminopyridine compound, selected from the group consisting of an acceptable salt thereof, that inhibits Aurora A and thus may be useful in cancer therapy.
priorityDate 2014-11-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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